The South African Health Products Regulatory Authority (SAHPRA), is the National Medicines Regulatory Authority established in terms of the Medicines and Related Substances Act, 1965, (Act No. 101 of 1965) as amended, to provide for the monitoring, evaluation, regulation, investigation, inspection, registration and control of medicines, scheduled substances,...
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Inspect different disciplines of pharmaceutical manufacturing, importing or exporting sites such as import/export/applicant and non-sterile manufacturing for compliance with Good Manufacturing Practices as accepted by SAHPRA.
Inspect non-sterile pharmaceutical testing laboratories (chemical and microbiological) for compliance with Good Manufacturing Practices as accepted by SAHPRA.
Planning of GMP inspections as per the inspection plan and travel arrangements for local, national and international inspections.
To work closely across inspection teams, SAHPRA programmes and external regulators to ensure inspection activities are planned and communicated effectively.
To adhere to the SAPRHA QMS processes
Qualification :
Applicants must have a Matric certificate and an appropriate four-year Bachelor of Pharmacy degree or Honours Degree in Chemistry or equivalent Health Science related qualification NQF level 8 as recognised by the South African Qualifications Authority (SAQA).
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